scholarly journals Phenotypical heterogeneity of mitochondrial encephalopathy with lactic acidosis and stroke-like episodes in a patient with recurrent movement disorder

2021 ◽  
Vol 0 (0) ◽  
pp. 0-0
Author(s):  
Hyug-Gi Kim ◽  
Kyung Mi Lee
Keyword(s):  
Lactic Acidosis ◽  
Movement Disorder ◽  
Mitochondrial Encephalopathy

Late-onset Mitochondrial Encephalopathy, Lactic Acidosis, and Stroke-like Episodes Presenting With Auditory Agnosia

2019 ◽  
Vol 24 (3) ◽  
pp. 90-92 ◽  
Author(s):  
Kelsey Smith ◽  
Shannon Chiu ◽  
Christopher Hunt ◽  
Adithya Chandregowda ◽  
Dusica Babovic-Vuksanovic ◽  
...  
Keyword(s):  
Lactic Acidosis ◽  
Late Onset ◽  
Mitochondrial Encephalopathy ◽  
Auditory Agnosia

scholarly journals Atypical Strokes in a Young African American Male: A Case of Mitochondrial Encephalopathy Lactic Acidosis and Stroke-Like Episodes (MELAS) Syndrome

2011 ◽  
Vol 2011 ◽  
pp. 1-2
Author(s):  
Jully M. Sanchez ◽  
Judy Ann Tan ◽  
Dimitrios Farmakiotis ◽  
Vikas Aggarwal
Keyword(s):  
African American ◽  
Lactic Acidosis ◽  
Mitochondrial Myopathy ◽  
African American Male ◽  
Young Male ◽  
Melas Syndrome ◽  
Clinical Context ◽  
Mitochondrial Encephalopathy

Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) syndrome is a rare but important cause of stroke-like symptoms which can often be missed Thambisetty and Newman 2004. We describe a case of a young male presenting with stroke-like episodes, later diagnosed with MELAS in an attempt to improve the understanding about diagnosing MELAS in the appropriate clinical context.

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